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Laura Oliva Pérez

@lauraolivaprez

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Results-driven clinical research specialist with a passion for impact.

Spain

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What I'm looking for

I am looking for a role that allows me to lead clinical trials and contribute to innovative healthcare solutions.

I am a dedicated clinical research specialist with over seven years of experience in managing Phase I, II, and III clinical trials. My journey in clinical research has been driven by a strong passion for improving healthcare outcomes and ensuring the integrity of clinical data. Currently, I serve as an Oncology Clinical Trial Coordinator at Hospital Clinic de Barcelona, where I have successfully coordinated over 200 clinical trials, navigating complex regulatory audits and ensuring compliance with Good Clinical Practice (GCP) guidelines.

Throughout my career, I have collaborated with international teams to foster an audit-ready environment, implementing standard operating procedures that enhance the efficiency and effectiveness of clinical research projects. My experience includes managing regulatory documentation, conducting study procedures, and monitoring patient safety and data accuracy. I am committed to advancing clinical research and contributing to the development of innovative therapies that can significantly impact patient lives.

Experience

Work history, roles, and key accomplishments

Current

Oncology Clinical Trial Coordinator

Current

Hospital Clinic de Barcelona

Nov 2019 - Present (5 years 7 months)

Coordinated over 200 phase I, II, and III oncology clinical trials, ensuring compliance with regulatory standards. Developed regulatory documentation and collaborated with cross-functional teams to maintain an audit-ready environment. Successfully navigated regulatory audits and inspections.

Clinical Trials Regulatory Compliance Data Management Cross Functional Collaboration Oncology

Traumatology Clinical Trial Coordinator

Hospital Mutua de Terrassa

Jan 2018 - Jan 2020 (1 year 11 months)

Managed and coordinated all aspects of over 50 device clinical trials. Submitted regulatory documents and monitored patient enrollment and data accuracy. Worked closely with auditors to resolve findings and implement corrective actions.

Device Trials Team Coordination

Intern - ctDNA Analysis

Institut Hospital del Mar d’Investigacions Mèdiques

Jan 2017 - Feb 2017 (1 month)

Conducted analysis of ctDNA in breast cancer as part of an internship program. Gained hands-on experience in molecular research techniques and contributed to ongoing studies.

Breast Cancer Research Research Collaboration

Intern - SRPX2 Expression Study

A.I. Virtanen Institute for Molecular Sciences

Jan 2016 - Feb 2016 (1 month)

Participated in a research internship focused on the expression of SRPX2 in uPA/uPAR knock-out mice. Developed skills in molecular biology and experimental design.

Experimental Design Research Techniques Data Analysis

Education

Degrees, certifications, and relevant coursework

Universitat Pompeu Fabra

Master in Clinical Research and Translational Oncology, Clinical Research

2016 - 2017

Completed a Master's degree in Clinical Research and Translational Oncology, focusing on the methodologies and practices essential for conducting clinical research and translating findings into clinical applications.

Universitat de Barcelona

Bachelor Degree in Molecular Biology, Molecular Biology

2012 - 2016

Earned a Bachelor's degree in Molecular Biology, covering various aspects of biological sciences, including genetics, biochemistry, and cellular biology.